WO2005067901A3 - Methodes permettant de traiter et de prevenir l'hypertension et les troubles associes a l'hypertension - Google Patents
Methodes permettant de traiter et de prevenir l'hypertension et les troubles associes a l'hypertension Download PDFInfo
- Publication number
- WO2005067901A3 WO2005067901A3 PCT/US2005/000677 US2005000677W WO2005067901A3 WO 2005067901 A3 WO2005067901 A3 WO 2005067901A3 US 2005000677 W US2005000677 W US 2005000677W WO 2005067901 A3 WO2005067901 A3 WO 2005067901A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- hypertension
- treating
- methods
- related disorders
- preventing
- Prior art date
Links
- 206010020772 Hypertension Diseases 0.000 title abstract 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA002552664A CA2552664A1 (fr) | 2004-01-08 | 2005-01-07 | Methodes permettant de traiter et de prevenir l'hypertension et les troubles associes a l'hypertension |
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US53541204P | 2004-01-08 | 2004-01-08 | |
US60/535,412 | 2004-01-08 | ||
US54710704P | 2004-02-24 | 2004-02-24 | |
US60/547,107 | 2004-02-24 | ||
US54862004P | 2004-02-27 | 2004-02-27 | |
US60/548,620 | 2004-02-27 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2005067901A2 WO2005067901A2 (fr) | 2005-07-28 |
WO2005067901A3 true WO2005067901A3 (fr) | 2005-12-01 |
Family
ID=34799611
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2005/000677 WO2005067901A2 (fr) | 2004-01-08 | 2005-01-07 | Methodes permettant de traiter et de prevenir l'hypertension et les troubles associes a l'hypertension |
Country Status (3)
Country | Link |
---|---|
US (1) | US20050239809A1 (fr) |
CA (1) | CA2552664A1 (fr) |
WO (1) | WO2005067901A2 (fr) |
Cited By (36)
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US8440677B2 (en) | 2009-03-24 | 2013-05-14 | Gilead Calistoga Llc | Atropisomers of 2-purinyl-3-tolyl-quinazolinone derivatives and methods of use |
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US8546409B2 (en) | 2009-04-20 | 2013-10-01 | Gilead Calistoga Llc | Methods of treatment for solid tumors |
US8569323B2 (en) | 2009-07-15 | 2013-10-29 | Intellikine, Llc | Substituted isoquinolin-1(2H)-one compounds, compositions, and methods thereof |
USRE44599E1 (en) | 2004-05-13 | 2013-11-12 | Icos Corporation | Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta |
US8604032B2 (en) | 2010-05-21 | 2013-12-10 | Infinity Pharmaceuticals, Inc. | Chemical compounds, compositions and methods for kinase modulation |
US8637542B2 (en) | 2008-03-14 | 2014-01-28 | Intellikine, Inc. | Kinase inhibitors and methods of use |
US8642604B2 (en) | 2006-04-04 | 2014-02-04 | The Regents Of The University Of California | Substituted pyrazolo[3,2-d]pyrimidines as anti-cancer agents |
US8691829B2 (en) | 2009-07-21 | 2014-04-08 | Gilead Calistoga Llc | Treatment of liver disorders with PI3K inhibitors |
US8697709B2 (en) | 2008-10-16 | 2014-04-15 | The Regents Of The University Of California | Fused ring heteroaryl kinase inhibitors |
US8703777B2 (en) | 2008-01-04 | 2014-04-22 | Intellikine Llc | Certain chemical entities, compositions and methods |
US8703778B2 (en) | 2008-09-26 | 2014-04-22 | Intellikine Llc | Heterocyclic kinase inhibitors |
US8785470B2 (en) | 2011-08-29 | 2014-07-22 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
US8785454B2 (en) | 2009-05-07 | 2014-07-22 | Intellikine Llc | Heterocyclic compounds and uses thereof |
US8809349B2 (en) | 2011-01-10 | 2014-08-19 | Infinity Pharmaceuticals, Inc. | Processes for preparing isoquinolinones and solid forms of isoquinolinones |
US8828998B2 (en) | 2012-06-25 | 2014-09-09 | Infinity Pharmaceuticals, Inc. | Treatment of lupus, fibrotic conditions, and inflammatory myopathies and other disorders using PI3 kinase inhibitors |
US8865730B2 (en) | 2012-03-05 | 2014-10-21 | Gilead Calistoga Llc | Polymorphic forms of (S)-2-(1-(9H-purin-6-ylamino)propyl)-5-fluoro-3-phenylquinazolin-4(3H)-one |
US8901133B2 (en) | 2010-11-10 | 2014-12-02 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
US8940742B2 (en) | 2012-04-10 | 2015-01-27 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
US8969363B2 (en) | 2011-07-19 | 2015-03-03 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
US8980899B2 (en) | 2009-10-16 | 2015-03-17 | The Regents Of The University Of California | Methods of inhibiting Ire1 |
US8993580B2 (en) | 2008-03-14 | 2015-03-31 | Intellikine Llc | Benzothiazole kinase inhibitors and methods of use |
US9056877B2 (en) | 2011-07-19 | 2015-06-16 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
US9096611B2 (en) | 2008-07-08 | 2015-08-04 | Intellikine Llc | Kinase inhibitors and methods of use |
US9238070B2 (en) | 2008-11-13 | 2016-01-19 | Gilead Calistoga Llc | Therapies for hematologic malignancies |
US9295673B2 (en) | 2011-02-23 | 2016-03-29 | Intellikine Llc | Combination of mTOR inhibitors and P13-kinase inhibitors, and uses thereof |
US9321772B2 (en) | 2011-09-02 | 2016-04-26 | The Regents Of The University Of California | Substituted pyrazolo[3,4-D]pyrimidines and uses thereof |
US9359365B2 (en) | 2013-10-04 | 2016-06-07 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
US9359349B2 (en) | 2007-10-04 | 2016-06-07 | Intellikine Llc | Substituted quinazolines as kinase inhibitors |
US9481667B2 (en) | 2013-03-15 | 2016-11-01 | Infinity Pharmaceuticals, Inc. | Salts and solid forms of isoquinolinones and composition comprising and methods of using the same |
US9487772B2 (en) | 2000-04-25 | 2016-11-08 | Icos Corporation | Inhibitors of human phosphatidylinositol 3-kinase delta |
US9492449B2 (en) | 2008-11-13 | 2016-11-15 | Gilead Calistoga Llc | Therapies for hematologic malignancies |
US9512125B2 (en) | 2004-11-19 | 2016-12-06 | The Regents Of The University Of California | Substituted pyrazolo[3.4-D] pyrimidines as anti-inflammatory agents |
US9708348B2 (en) | 2014-10-03 | 2017-07-18 | Infinity Pharmaceuticals, Inc. | Trisubstituted bicyclic heterocyclic compounds with kinase activities and uses thereof |
US10131668B2 (en) | 2012-09-26 | 2018-11-20 | The Regents Of The University Of California | Substituted imidazo[1,5-a]pYRAZINES for modulation of IRE1 |
US10160761B2 (en) | 2015-09-14 | 2018-12-25 | Infinity Pharmaceuticals, Inc. | Solid forms of isoquinolinones, and process of making, composition comprising, and methods of using the same |
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WO2005016348A1 (fr) * | 2003-08-14 | 2005-02-24 | Icos Corporation | Methodes d'inhibition de reponses immunes stimulees par un facteur endogene |
CA2563038C (fr) | 2004-04-02 | 2013-10-29 | Gaik Beng Kok | Composes neurologiquement actifs |
CA2730540A1 (fr) * | 2004-05-13 | 2005-12-01 | Vanderbilt University | Inhibiteurs selectifs de la phosphoinositide-3-kinase delta pour inhiber l'angiogenese |
CA2598409A1 (fr) * | 2005-02-17 | 2006-08-24 | Icos Corporation | Procede d'inhibition d'accumulation de leucocytes |
BRPI0609509A2 (pt) | 2005-03-30 | 2010-04-13 | Conforma Therapeutics Corp | composto ou um polimorfo, solvato, tautÈmero, enanciÈmero, pró-droga ou sal farmaceuticamente aceitável do mesmo, composição farmacêutica, e, uso do composto, polimorfo, solvato, tautÈmero, enanciÈmero, pró-droga ou sal farmaceuticamente aceitável |
EP2079739A2 (fr) | 2006-10-04 | 2009-07-22 | Pfizer Products Inc. | Dérivés de pyrido[4,3-d]pyrimidin-4(3h)-one utilisés en tant qu'antagonistes du récepteur calcique |
EA024359B1 (ru) | 2007-06-29 | 2016-09-30 | Джилид Сайэнс, Инк. | Пуриновые производные и их применение в качестве модуляторов толл-подобного рецептора 7 |
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US20110294803A1 (en) * | 2008-12-04 | 2011-12-01 | Law Amanda J | Phosphatidylinositol-3-kinase p110 delta-targeted drugs in the treatment of cns disorders |
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UY33337A (es) | 2010-10-18 | 2011-10-31 | Respivert Ltd | DERIVADOS SUSTITUIDOS DE 1H-PIRAZOL[ 3,4-d]PIRIMIDINA COMO INHIBIDORES DE LAS FOSFOINOSITIDA 3-QUINASAS |
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JP6584952B2 (ja) | 2012-11-01 | 2019-10-02 | インフィニティー ファーマシューティカルズ, インコーポレイテッド | Pi3キナーゼアイソフォームモジュレーターを用いる癌の治療 |
TW201522341A (zh) | 2013-03-15 | 2015-06-16 | Respivert Ltd | 化合物 |
US9227977B2 (en) | 2013-03-15 | 2016-01-05 | Respivert Ltd. | Phosphoinositide 3-kinase inhibitors |
UY35675A (es) | 2013-07-24 | 2015-02-27 | Novartis Ag | Derivados sustituidos de quinazolin-4-ona |
WO2015051241A1 (fr) | 2013-10-04 | 2015-04-09 | Infinity Pharmaceuticals, Inc. | Composés hétérocycliques et leurs utilisations |
EP3083623A1 (fr) | 2013-12-20 | 2016-10-26 | Gilead Calistoga LLC | Formes polymorphes d'un sel chlorhydrate de la (s)-2-(9h-purine-6-ylamino)propyl)-5-fluoro-3-phénylquinazolin-4(3h)-one |
WO2015095601A1 (fr) | 2013-12-20 | 2015-06-25 | Gilead Calistoga Llc | Procédés de synthèse d'inhibiteurs de la phosphatidylinositol 3-kinase |
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US20150320755A1 (en) | 2014-04-16 | 2015-11-12 | Infinity Pharmaceuticals, Inc. | Combination therapies |
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KR20170082490A (ko) | 2014-07-04 | 2017-07-14 | 루핀 리미티드 | Pi3k 억제제로서 퀴놀리지논 유도체 |
CN106714800B (zh) | 2014-07-11 | 2021-09-03 | 吉利德科学公司 | 用于治疗hiv的toll样受体调节剂 |
KR20170054481A (ko) | 2014-09-16 | 2017-05-17 | 길리애드 사이언시즈, 인코포레이티드 | 톨-유사 수용체 조정제의 고체 형태 |
EP3317277B1 (fr) | 2015-07-01 | 2021-01-20 | Crinetics Pharmaceuticals, Inc. | Modulateurs de la somatostatine et leurs utilisations |
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WO2017161116A1 (fr) | 2016-03-17 | 2017-09-21 | Infinity Pharmaceuticals, Inc. | Isotopologues de composés isoquinolinone et quinazolinone et leurs utilisations comme inhibiteurs de la kinase pi3k |
WO2017214269A1 (fr) | 2016-06-08 | 2017-12-14 | Infinity Pharmaceuticals, Inc. | Composés hétérocycliques et leurs utilisations |
KR20190033526A (ko) | 2016-06-24 | 2019-03-29 | 인피니티 파마슈티칼스, 인코포레이티드 | 병용 요법 |
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Citations (5)
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WO2001081346A2 (fr) * | 2000-04-25 | 2001-11-01 | Icos Corporation | Inhibiteurs de la phosphatidyl-inositol 3-kinase delta humaine |
WO2003035075A1 (fr) * | 2001-10-19 | 2003-05-01 | Icos Corporation | Inhibiteurs de phosphatidyl-inositol 3-kinase delta |
WO2005016349A1 (fr) * | 2003-08-14 | 2005-02-24 | Icos Corporation | Methodes d'inhibition de l'accumulation des leucocytes |
WO2005016348A1 (fr) * | 2003-08-14 | 2005-02-24 | Icos Corporation | Methodes d'inhibition de reponses immunes stimulees par un facteur endogene |
WO2005042519A1 (fr) * | 2003-10-31 | 2005-05-12 | Warner-Lambert Company Llc | Pyrimidines a titre d'inhibiteurs de phosphoinositide-3-kinases (pi3k) |
Family Cites Families (2)
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US5869040A (en) * | 1995-06-07 | 1999-02-09 | Biogen, Inc | Gene therapy methods and compositions |
US5858753A (en) * | 1996-11-25 | 1999-01-12 | Icos Corporation | Lipid kinase |
-
2005
- 2005-01-07 US US11/031,477 patent/US20050239809A1/en not_active Abandoned
- 2005-01-07 CA CA002552664A patent/CA2552664A1/fr not_active Abandoned
- 2005-01-07 WO PCT/US2005/000677 patent/WO2005067901A2/fr active Application Filing
Patent Citations (5)
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WO2001081346A2 (fr) * | 2000-04-25 | 2001-11-01 | Icos Corporation | Inhibiteurs de la phosphatidyl-inositol 3-kinase delta humaine |
WO2003035075A1 (fr) * | 2001-10-19 | 2003-05-01 | Icos Corporation | Inhibiteurs de phosphatidyl-inositol 3-kinase delta |
WO2005016349A1 (fr) * | 2003-08-14 | 2005-02-24 | Icos Corporation | Methodes d'inhibition de l'accumulation des leucocytes |
WO2005016348A1 (fr) * | 2003-08-14 | 2005-02-24 | Icos Corporation | Methodes d'inhibition de reponses immunes stimulees par un facteur endogene |
WO2005042519A1 (fr) * | 2003-10-31 | 2005-05-12 | Warner-Lambert Company Llc | Pyrimidines a titre d'inhibiteurs de phosphoinositide-3-kinases (pi3k) |
Non-Patent Citations (3)
Title |
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DREES B E ET AL: "Therapeutic potential of phosphoinositide 3-kinase inhibitors", EXPERT OPINION ON THERAPEUTIC PATENTS 2004 UNITED KINGDOM, vol. 14, no. 5, 2004, pages 703 - 732, XP002346345, ISSN: 1354-3776 * |
NORTHCOTT CARRIE A ET AL: "PI3-kinase upregulation and involvement in spontaneous tone in arteries from DOCA-salt rats: is p110delta the culprit?", HYPERTENSION. APR 2004, vol. 43, no. 4, April 2004 (2004-04-01), pages 885 - 890, XP002346346, ISSN: 1524-4563 * |
WARD STEPHEN G ET AL: "Isoform-specific phosphoinositide 3-kinase inhibitors as therapeutic agents.", CURRENT OPINION IN PHARMACOLOGY. AUG 2003, vol. 3, no. 4, August 2003 (2003-08-01), pages 426 - 434, XP002346297, ISSN: 1471-4892 * |
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---|---|---|---|---|
US9487772B2 (en) | 2000-04-25 | 2016-11-08 | Icos Corporation | Inhibitors of human phosphatidylinositol 3-kinase delta |
US8993583B2 (en) | 2004-05-13 | 2015-03-31 | Icos Corporation | 5-fluoro-3-phenyl-2-[1-(9H-purin-6-ylamino)propyl]-3H-quinazolin-4-one and 6-fluoro-3-phenyl-2-[1-(9H-purin-6-ylamino)ethyl]-3H-quinazolin-4-one as inhibitors of human phosphatidylinositol 3-kinase delta |
USRE44638E1 (en) | 2004-05-13 | 2013-12-10 | Icos Corporation | Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta |
US9149477B2 (en) | 2004-05-13 | 2015-10-06 | Icos Corporation | 5-fluoro-3-phenyl-2-[1-(9h-purin-6-ylamino)propyl]-3h-quinazolin-4-one as an inhibitor of human phosphatidylinositol 3-kinase delta |
US8779131B2 (en) | 2004-05-13 | 2014-07-15 | Icos Corporation | 6-fluoro-3-phenyl-2-[1-(9H-purin-6-ylamino)-ethyl]-3H-quinazolin-4-one as an inhibitor of human phosphatidylinositol 3-kinase delta |
USRE44599E1 (en) | 2004-05-13 | 2013-11-12 | Icos Corporation | Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta |
US8586597B2 (en) | 2004-05-13 | 2013-11-19 | Icos Corporation | 6-fluoro-3-phenyl-2-[1-(9H-purin-6-ylamino)ethyl]-3H-quinazolin-4-one as an inhibitor of human phosphatidylinositol 3-kinase delta |
US8980901B2 (en) | 2004-05-13 | 2015-03-17 | Icos Corporation | 5-fluoro-3-phenyl-2[1-(9H-purin-6-ylamino)propyl]-3H-quinazolin-4-one and 6-fluoro-3-phenyl-2-[1-(9H-purin-6-ylamino)ethyl]-3H-quinazolin-4-one as inhibitors of human phosphatidylinositol 3-kinase delta |
US9512125B2 (en) | 2004-11-19 | 2016-12-06 | The Regents Of The University Of California | Substituted pyrazolo[3.4-D] pyrimidines as anti-inflammatory agents |
US9493467B2 (en) | 2006-04-04 | 2016-11-15 | The Regents Of The University Of California | PI3 kinase antagonists |
US8642604B2 (en) | 2006-04-04 | 2014-02-04 | The Regents Of The University Of California | Substituted pyrazolo[3,2-d]pyrimidines as anti-cancer agents |
US9359349B2 (en) | 2007-10-04 | 2016-06-07 | Intellikine Llc | Substituted quinazolines as kinase inhibitors |
US8785456B2 (en) | 2008-01-04 | 2014-07-22 | Intellikine Llc | Substituted isoquinolin-1(2H)-ones, and methods of use thereof |
US9216982B2 (en) | 2008-01-04 | 2015-12-22 | Intellikine Llc | Certain chemical entities, compositions and methods |
US8703777B2 (en) | 2008-01-04 | 2014-04-22 | Intellikine Llc | Certain chemical entities, compositions and methods |
US9655892B2 (en) | 2008-01-04 | 2017-05-23 | Intellikine Llc | Certain chemical entities, compositions and methods |
US8637542B2 (en) | 2008-03-14 | 2014-01-28 | Intellikine, Inc. | Kinase inhibitors and methods of use |
US9637492B2 (en) | 2008-03-14 | 2017-05-02 | Intellikine Llc | Benzothiazole kinase inhibitors and methods of use |
US8993580B2 (en) | 2008-03-14 | 2015-03-31 | Intellikine Llc | Benzothiazole kinase inhibitors and methods of use |
US9096611B2 (en) | 2008-07-08 | 2015-08-04 | Intellikine Llc | Kinase inhibitors and methods of use |
US8703778B2 (en) | 2008-09-26 | 2014-04-22 | Intellikine Llc | Heterocyclic kinase inhibitors |
US9296742B2 (en) | 2008-09-26 | 2016-03-29 | Intellikine Llc | Heterocyclic kinase inhibitors |
US8697709B2 (en) | 2008-10-16 | 2014-04-15 | The Regents Of The University Of California | Fused ring heteroaryl kinase inhibitors |
US8476431B2 (en) | 2008-11-03 | 2013-07-02 | Itellikine LLC | Benzoxazole kinase inhibitors and methods of use |
US8476282B2 (en) | 2008-11-03 | 2013-07-02 | Intellikine Llc | Benzoxazole kinase inhibitors and methods of use |
US9238070B2 (en) | 2008-11-13 | 2016-01-19 | Gilead Calistoga Llc | Therapies for hematologic malignancies |
US9492449B2 (en) | 2008-11-13 | 2016-11-15 | Gilead Calistoga Llc | Therapies for hematologic malignancies |
US10154998B2 (en) | 2008-11-13 | 2018-12-18 | Gilead Calistoga Llc | Therapies for hematologic malignancies |
US8440677B2 (en) | 2009-03-24 | 2013-05-14 | Gilead Calistoga Llc | Atropisomers of 2-purinyl-3-tolyl-quinazolinone derivatives and methods of use |
US8546409B2 (en) | 2009-04-20 | 2013-10-01 | Gilead Calistoga Llc | Methods of treatment for solid tumors |
US8785454B2 (en) | 2009-05-07 | 2014-07-22 | Intellikine Llc | Heterocyclic compounds and uses thereof |
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US20050239809A1 (en) | 2005-10-27 |
CA2552664A1 (fr) | 2005-07-28 |
WO2005067901A2 (fr) | 2005-07-28 |
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